“…Flusilazole, like other triazole fungicides acts by interrupting the formation of fungal cell walls through inhibition of sterol-14α-demethylase (CYP51), which is highly conserved across taxa including animals, where it is utilised in the pathway to cholesterol formation; thus effects on cell membranes may not be restricted to the target species (Bossche et al, 1995;Zarn et al, 2003). The hazards posed by triazoles to wildlife is because their effects may not be limited to CYP51, and there is emerging evidence that they may accumulate in the tissues of amphibians, (Hansen et al, 2014;Poulsen et al, 2015;Smalling et al, 2013), although this may vary depending on the levels found in the environment (Smalling et al, 2015). At low levels of exposure, triazole fungicides have been associated with endocrine disruption, disrupting steroidogenesis in adult male frogs at concentrations as low as 1 µg/L (Poulsen et al, 2015), as well as developmental defects in tadpoles and embryos (Bernabò et al, 2016;Di Renzo et al, 2011;Groppelli et al, 2005;Papis et al, 2006).…”